Canonical Allele Identifier: CA1604713970

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603347G= , CM000667.2:g.180603347G=	GRCh38
NC_000005.9:g.180030347G= , CM000667.1:g.180030347G=	GRCh37
NC_000005.8:g.179962953G=	NCBI36
NG_011536.1:g.51278C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3937C= MANE Select	ENSP00000261937.6:p.Pro1313=
ENST00000261937.10:c.3937C=	ENSP00000261937.6:p.Pro1313=
ENST00000502603.5:n.637C=
NM_182925.4:c.3937C=	NP_891555.2:p.Pro1313=
XM_011534477.1:c.4186C=	XP_011532779.1:p.Pro1396=
XM_011534478.1:c.4168C=	XP_011532780.1:p.Pro1390=
XM_011534479.1:c.*83C=	XP_011532781.1:n.*83C=
XM_011534482.1:c.3955C=	XP_011532784.1:p.Pro1319=
XM_011534483.1:c.3877C=	XP_011532785.1:p.Pro1293=
XM_011534484.1:c.3478C=	XP_011532786.1:p.Pro1160=
XR_941095.1:n.4223C=
XM_011534478.3:c.4168C=	XP_011532780.1:p.Pro1390=
XM_011534484.2:c.3478C=	XP_011532786.1:p.Pro1160=
XM_017009263.1:c.*83C=	XP_016864752.1:n.*83C=
XM_017009268.1:c.3859C=	XP_016864757.1:p.Pro1287=
XR_001742050.2:n.4427C=
NM_182925.5:c.3937C= MANE Select	NP_891555.2:p.Pro1313=